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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752236Generated: October 28, 2026

tert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate → Tert-butyl 4-(4-methoxy-3-methylbenzoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1752236

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylateHCID 11065582—
ReactantHCID 178491913HCID 178491913—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(4-methoxy-3-methylbenzoyl)piperidine-1-carboxylateHCID 7121219599%

Reaction Steps

To a solution of 4-(methoxy-methyl-carbamoyl)-piperidine-1-carboxylic acid tert-butyl ester (5.0 g, 18.36 mmol) in 50 mL dry THF at ambient temperature was added (4-methoxy-3-methylphenyl)magnesium bromide (55.1 mL, 0.5 M) was added dropwise under N2, the reaction mixture was stirred at the same temperature for 16 hours. The reaction was quenched with saturated sodium sulfate solution (10 mL) and partitioned between brine (150 mL) and 10% isopropyl alcohol/chloroform (200 mL), and the organic layer was removed to yield the crude product. Purification by flash chromatography (silica: 5-35% ethyl acetate/pentane) gave the title compound as a white solid (6.4 g, 19.21 mmol, >99% yield). HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 10-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) retention time=4.131 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163003B2
Source datasetuspto-grants-2015_10
ORD IDord-4fed1aa347e04fb6b9d445d76dc1fc86
Source noteuspto-grants-2015_10